Package 51655-605-26
Brand: citalopram
Generic: citalopram hydrobromidePackage Facts
Identity
Package NDC
51655-605-26
Digits Only
5165560526
Product NDC
51655-605
Description
90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-605-26)
Marketing
Marketing Status
Brand
citalopram
Generic
citalopram hydrobromide
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "494f25f9-6036-798e-e063-6294a90ab59f", "openfda": {"unii": ["I1E9D14F36"], "rxcui": ["283672"], "spl_set_id": ["d9cc1649-913d-832d-e053-2995a90a5f9a"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-605-26)", "package_ndc": "51655-605-26", "marketing_start_date": "20220302"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-605-52)", "package_ndc": "51655-605-52", "marketing_start_date": "20210401"}], "brand_name": "Citalopram", "product_id": "51655-605_494f25f9-6036-798e-e063-6294a90ab59f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "51655-605", "generic_name": "Citalopram Hydrobromide", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Citalopram", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "10 mg/1"}], "application_number": "ANDA077031", "marketing_category": "ANDA", "marketing_start_date": "20210401", "listing_expiration_date": "20271231"}